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Trifluoroacetic acid → HCID 178484795, 화합물

HRID 25614
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HRID 25614 반응식
[CH3:1][NH:2][C@H:3]1[CH2:8][CH2:7][C@H:6]([CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]OS(C)(=O)=O)[CH2:5][CH2:4]1.FC(F)(F)C(O)=O.[F:26][C:27]([F:39])([F:38])[C:28]1[CH:33]=[CH:32][C:31]([S:34](Cl)(=[O:36])=[O:35])=[CH:30][CH:29]=1.[OH:40][CH2:41][CH2:42][NH:43][CH2:44][CH2:45][OH:46]>>[OH:40][CH2:41][CH2:42][N:43]([CH2:44][CH2:45][OH:46])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][C@H:6]1[CH2:5][CH2:4][C@H:3]([N:2]([CH3:1])[S:34]([C:31]2[CH:32]=[CH:33][C:28]([C:27]([F:39])([F:38])[F:26])=[CH:29][CH:30]=2)(=[O:36])=[O:35])[CH2:8][CH2:7]1
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HCID 6422Trifluoroacetic acidHCID 8113DiethanolamineHCID 27773994-(Trifluoromethyl)benzenesulfonyl chlorideHCID 178484796HCID 178484796, 화합물

생성물 1

HCID 178484795HCID 178484795, 화합물

실험 절차

In analogy to examples 29.10 and 29.11, trans-Methansulfonic acid 5-(4-methyl amino-cyclohexyl)-pentyl ester.trifluoroacetic acid salt and 4-trifluoromethyl-phenyl sulfonylchloride were reacted) followed by treatment with 2-(2-Hydroxy-ethylamino)-ethanol to give trans-N-(4-{5-[Bis-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide. MS: 495 (MH+).

출처 및 근거

ORD 기록
ord-807a9fec619941e58097b08948ea1137
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06858651B2

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